Manifestation of Huntington's disease pathology in human induced pluripotent stem cell-derived neurons

© 2016 Nekrasov et al.Background: Huntington's disease (HD) is an incurable hereditary neurodegenerative disorder, which manifests itself as a loss of GABAergic medium spiny (GABA MS) neurons in the striatum and caused by an expansion of the CAG repeat in exon 1 of the huntingtin gene. There is no cure for HD, existing pharmaceutical can only relieve its symptoms. Results: Here, induced pluripotent stem cells were established from patients with low CAG repeat expansion in the huntingtin gene, and were then efficiently differentiated into GABA MS-like neurons (GMSLNs) under defined culture conditions. The generated HD GMSLNs recapitulated disease pathology in vitro, as evidenced by mutant huntingtin protein aggregation, increased number of lysosomes/autophagosomes, nuclear indentations, and enhanced neuronal death during cell aging. Moreover, store-operated channel (SOC) currents were detected in the differentiated neurons, and enhanced calcium entry was reproducibly demonstrated in all HD GMSLNs genotypes. Additionally, the quinazoline derivative, EVP4593, reduced the number of lysosomes/autophagosomes and SOC currents in HD GMSLNs and exerted neuroprotective effects during cell aging. Conclusions: Our data is the first to demonstrate the direct link of nuclear morphology and SOC calcium deregulation to mutant huntingtin protein expression in iPSCs-derived neurons with disease-mimetic hallmarks, providing a valuable tool for identification of candidate anti-HD drugs. Our experiments demonstrated that EVP4593 may be a promising anti-HD drug

Dominant Effect of Full-Length Presenilin-1 on the Enhancement of Store-Operated Calcium Entry

Most of the cases of the Alzheimer's disease are linked with mutations in presenilin-1 (PS1) gene. Normally PS1 is cleaved to terminal fragments, which comprise catalytic core of gamma-secretase. Considerable portion of the mutations in PS1 gene disrupts PS1 endoproteolysis and subsequent holoprotein accumulation. One of those mutations is a deletion of 9th exon of the PS1 gene. In this study we demonstrate that the PS1 holoprotein enhanced store-operated calcium (SOC) entry independently of its terminal fragments. Moreover, we demonstrate that the increase in SOC entry was caused by holoprotein independently of its enzyme activity. Expressions of the PS1 C- or N-terminal fragments did not have any effect on SOC entry. At the same time, the N-terminal fragment co-expression with PS1 mutants was able to reduce their effects on SOC only slightly, due to the probable competition for the same molecular target. Overall, our data demonstrate that an increase in the SOC entry is caused by a dominant effect of the PS1 holoprotein accumulation independently of gamma-secretase activity of PS1 and A beta production.Peer reviewe

Suppression of TRPC3 leads to disappearance of store-operated channels and formation of a new type of store-independent channels in A431 cells.

In most non-excitable cells, calcium (Ca(2+)) release from the inositol 1,4,5-trisphosphate (InsP(3))-sensitive intracellular Ca(2+) stores is coupled to Ca(2+) influx through the plasma membrane Ca(2+) channels whose molecular composition is poorly understood. Several members of mammalian TRP-related protein family have been implicated to both receptor- and store-operated Ca(2+) influx. Here we investigated the role of the native transient receptor potential 3 (TRPC3) homologue in mediating the store- and receptor-operated calcium entry in A431 cells. We show that suppression of TRPC3 protein levels by small interfering RNA (siRNA) leads to a significant reduction in store-operated calcium influx without affecting the receptor-operated calcium influx. With single-channel analysis, we further demonstrate that reduction of TRPC3 levels results in suppression of specific subtype of store-operated calcium channels and activation of store-independent channels. Our data suggest that TRPC3 is required for the formation of functional store-operated channels in A431 cells

MEDICO-GENETIC ASPECTS OF INFERTILITY

Results of medico-genetic examination of 304 married couples with infertility (608 individuals) are presented in article. Frequency of genetic abnormalities and infertility structure are revealed. Comparative analysis between 2 groups of couples with male as well as combined infertility is performed. The groups were formed according the results of infertility treatment using methods of ART. The factors having had statistically significant impact on fertility were revealed

Manifestation of Huntington's disease pathology in human induced pluripotent stem cell-derived neurons

© 2016 Nekrasov et al.Background: Huntington's disease (HD) is an incurable hereditary neurodegenerative disorder, which manifests itself as a loss of GABAergic medium spiny (GABA MS) neurons in the striatum and caused by an expansion of the CAG repeat in exon 1 of the huntingtin gene. There is no cure for HD, existing pharmaceutical can only relieve its symptoms. Results: Here, induced pluripotent stem cells were established from patients with low CAG repeat expansion in the huntingtin gene, and were then efficiently differentiated into GABA MS-like neurons (GMSLNs) under defined culture conditions. The generated HD GMSLNs recapitulated disease pathology in vitro, as evidenced by mutant huntingtin protein aggregation, increased number of lysosomes/autophagosomes, nuclear indentations, and enhanced neuronal death during cell aging. Moreover, store-operated channel (SOC) currents were detected in the differentiated neurons, and enhanced calcium entry was reproducibly demonstrated in all HD GMSLNs genotypes. Additionally, the quinazoline derivative, EVP4593, reduced the number of lysosomes/autophagosomes and SOC currents in HD GMSLNs and exerted neuroprotective effects during cell aging. Conclusions: Our data is the first to demonstrate the direct link of nuclear morphology and SOC calcium deregulation to mutant huntingtin protein expression in iPSCs-derived neurons with disease-mimetic hallmarks, providing a valuable tool for identification of candidate anti-HD drugs. Our experiments demonstrated that EVP4593 may be a promising anti-HD drug